ZMP
zgc:171872
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC100141342 [Source:RefSeq peptide;Acc:NP_001108379]
Human Orthologue:
KCNQ2
Human Description:
potassium voltage-gated channel, KQT-like subfamily, member 2 [Source:HGNC Symbol;Acc:6296]
Mouse Orthologue:
Kcnq2
Mouse Description:
potassium voltage-gated channel, subfamily Q, member 2 Gene [Source:MGI Symbol;Acc:MGI:1309503]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa44687 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa21297 | Nonsense | Available for shipment | Available now |
| sa492 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa44687
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000113492 | Nonsense | 166 | 349 | 3 | 7 |
| ENSDART00000131736 | Nonsense | 166 | 883 | 3 | 18 |
Genomic Location (Zv9):
Chromosome 8 (position 26257675)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 25385593 |
| GRCz11 | 8 | 25404732 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTGCTGCTGTCGCTACAGAGGATGGAGAGGAAGGCTGAGATTTGCTCGC[A/T]AACCCTTCTGTATCATCGGTTAGAAAATCATCTGCTCTCTTTCTTTGTGC
Long Flanking Sequence:
TACAATAACTTGCCTAATTACCCTAACCTGCCTAGTTAACCTAATTAACCTAATTAACCTAGTTAAGCCTTTATATGTCACTAAACTGTTTAAAACTGTGTAAACTGTTTAGAAGTGTTTTTATATATCTTGAAAAATATATAGTGAAATATTATTTACTGTCGTCATGGCAAAGGCAAAATAAATCAGTTATTAGAAAGGAGTTAATAAAACTATTATGTTTAGAAATGTGTTAAAAAAATTCTCTCCGTTAAACAGAAATTGGGGGAAAAATAAACAGGGGGCTAATAATTCTGACATCAACTGTATGTTATTGGACATGTGAAATTAGGAAGCTCAAATAAATGGGACAATAACTGGATGTAAAAATAAAAGTGTGTGCTGTTTTCCAGGAAATTGTGACAATCGTGGTGTTTGGTGTGGAATATATTGTGCGTATCTGGGCTGCCGGCTGCTGCTGTCGCTACAGAGGATGGAGAGGAAGGCTGAGATTTGCTCGC[A/T]AACCCTTCTGTATCATCGGTTAGAAAATCATCTGCTCTCTTTCTTTGTGCCTGTTCTGATTTTCTTCTCTAATGCAAGTTTTTTTTCTCCTTTTTTCTCCACCGCTTTCTCTCTCTCGTTATTCTTCCTGCTCAAGAGACAATAAAATCTGCTTTGCCAACTTTTTTCTGGGGCAGTAAACGAGCAAAGGGTTGGCACTCTCTGAATTACGACACTTGATATGCCAGCGCTATACAGAAGAATAATGCAAACTCCATTAGTGCATGATTTGAAAGAAGAGATGATGCCAGTAAATATGAGATTGATAGTCAGATTAGTGAAACTATTCATTTAAAAATGACATTTCTGTCAGCATTTAATCACACTGATGTCATTCAAACATTGATAATTTTCTTCAACATTTCAGAACAATTAACTGTCCCTGTAAGAAACGCATTGTTTGCATAAACCATATGGAGAATATCTATATCATGTACAGTCAGGGATGGACAGTATTTATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21297
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000113492 | Nonsense | 223 | 349 | 4 | 7 |
| ENSDART00000131736 | Nonsense | 223 | 883 | 4 | 18 |
Genomic Location (Zv9):
Chromosome 8 (position 26252842)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 25380760 |
| GRCz11 | 8 | 25399899 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCGAATGCTGCGAATGGACCGGCGCGGTGGCACATGGAAGCTCCTGGGAT[C/A]AGTCGTCTATGCGCACAGCAAGGTGACTAATAACATGCTTGATTTTGTAT
Long Flanking Sequence:
TGATGTATTGTGCAGCTTTAAATCATACCTCTGGCAGATTCTGACTTAAACTTACTTTTATTCATCCAGCAAGATTTTTTTTCTGACCAGAAATAACAAAAGCTTTCCCAAAAGATAATAAGACCCTGTGGAAGAGGCATCATTGTGGAAGCTTTTAATAACTTTTTTACAAAAACAAAAAGAATTTGCCAGGGGTATGATTAATTTTGGGTTTAACTGTGTATGATATACATTTGGCGTGGTTCAAAAACATTGTTAATCAATAAATATATTATGTTTATGTAAAAATTAAGTTTATATTATGTTGGGGTTTTATGTGATAACTTAAACACACTCTTTATCTGCAGATATCATGGTGCTTTTCGCCTCGGTGTCTGTCCTGGCCGCTGGCTCACAGGGGAATGTTTTTGCCACCTCGGCCATAAGGAGTCTGAGGTTTCTCCAGATCCTCCGAATGCTGCGAATGGACCGGCGCGGTGGCACATGGAAGCTCCTGGGAT[C/A]AGTCGTCTATGCGCACAGCAAGGTGACTAATAACATGCTTGATTTTGTATTTTCTTTTTTTTTTGCACAATGACTGCATGTGTGTACTGCATGTTTACTGGATGTTCAAACTAAGAAAAAAAGGTTAGCTACATTACAGGTGCACTGTGGCATCTTAAAGGAAAATGTTTGTAACCGTAGGGAACACTTGACTAGGTACTATAATGTACACATTTGTACTTTTTAGGTATAGATATGTACCTTTAAGTTACAAATGTGGATCCCAGTGGCAGCTTTTATACCTTTATTTCTGAGCGAGTTATACATTAGAGTATATACAATTGTTTGTTCATATACTTATTAAACTTATACATATACTTATTTAACGCAAAGGTTAAACAGGTTATTAGAGTAAGTGAGCATGTTTCCACTGGTCTGCCATGGGTCAGTAGGCAGAAAATTTATTATTATTCATTCGTTTCTATTACTGGAAAAATGATATCACTCAATTTAGTCTATAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa492
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000113492 | None | None | 349 | None | 7 |
| ENSDART00000131736 | Nonsense | 384 | 883 | 9 | 18 |
Genomic Location (Zv9):
Chromosome 8 (position 26245699)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 25373617 |
| GRCz11 | 8 | 25392756 |
KASP Assay ID:
554-0179.1 (used for ordering genotyping assays)
KASP Sequence:
TTTTCCATTAGATTTCATTAAGCAGAAACACACTTCTCAGCAATTTATGG[C/T]AGTTTGATATGCTGTTGGTACTGTAGGCATTTAAAAGTCTGCTCCCCATC
Long Flanking Sequence:
CAGACTAATTTCTTATAATACATTTACTCACCTCAAAAGAAATCCGGAATGCAGTAAAAGGATGGATTAAAACAGCAGGTGTAAACATGAATCAGCAATATAATCCAACAGAAGTATTTTAATACCAGGTGTTAGCAGGGCTCTAGAATGATATGACTAAAAATGTTAATTACAGCATATACTTAATTATTCATCACTGTGAAGGTCATGAAAGTCAATTTCATTCATTTTTTCTTTCCCGTCAGGCTGCTTGGAGGTTTCATGCCACAAACCTATCACGAACAGACCTTTTTTCCACATGGGACTTTTATGCACAGACAGTGTCAGTCCCAATGTACAGGTAGTCAATCATCCTGAGGGCCATTGTGACTGTACAAGTTTTAATGAAATAGTTTTTAGTATGCTGTTTTTCTCTCAATTATAATATTTCTCAGTAGAGTTTGGAATATTTTTTCCATTAGATTTCATTAAGCAGAAACACACTTCTCAGCAATTTATGG[C/T]AGTTTGATATGCTGTTGGTACTGTAGGCATTTAAAAGTCTGCTCCCCATCCTCCCTTTTCCTATAGACTTATTCCTCCTGTAAATCAGCTGGACATTTTAAGAAGTCTGAAGGGAAAGTCTGCTTTCAGGTTGGTTATTATATCATTTAAATATGTATACAAGTAACACTGTACTATGATCACCATATCTGTCATATGACCACAAGAGTTAAAAATATAAGACCCAACTGTCAAAAATATGGATTTTTGTTTGAAGATAGAAATAAATCAAACATTTTAGAATTTGTAAAACGTTGTGGAAAAAAGTAGTCAGTCAGTACACACTGTAAAAGTATAGGGGTCCACGCTATTCCTTCATGTCGTCCCAAAGCAAATCAATTAAGTTAAGTTGATTGAAAATAAAACAATTTAGTTGCAGGAAGAAAACTCAATAATTGTGTTGTTTCACCTTATTTTATAGAAATAGTTTAAACAAACAGCAAAAAAAAAAAAAAAATCAC
Associated Phenotype:
Not determined